Chr Mutation (hg38) CAid Gene Transcript Linkouts
20g.4699533C>ACA123097PRNPc.313C>A (p.Pro105Thr)
c.*2C>A (n.*2C>A)
 ClinVar dbSNP
20g.4699533C>TCA256788PRNPc.313C>T (p.Pro105Ser)
c.*2C>T (n.*2C>T)
 ClinVar dbSNP gnomAD v2 gnomAD v4

Number of alleles fetched